# FDA Inspection 1069413 - KEDPlasma, LLC - September 19, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/kedplasma-llc/00c06619-00c6-40aa-8b52-90271813de79
Source feed: FDA_Inspections

> FDA Inspection 1069413 for KEDPlasma, LLC on September 19, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1069413
- Company Name: KEDPlasma, LLC
- Inspection Date: 2018-09-19
- Classification: No Action Indicated (NAI)
- Project Area: Blood and Blood Products
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

## Related Documents

- [FDA Inspection 966746 - 2016-01-26](https://www.globalkeysolutions.net/records/fda_inspections/kedplasma-llc/8942a537-3f55-4e54-a0bd-4132a89bde98)
- [FDA Inspection 683927 - 2010-09-15](https://www.globalkeysolutions.net/records/fda_inspections/kedplasma-llc/e1c52af8-d9b5-429a-8a6b-fb4ac6c7d448)

Company: https://www.globalkeysolutions.net/companies/kedplasma-llc/48c94355-8238-4245-97c0-e4c8d8b0b29c

Office: https://www.globalkeysolutions.net/offices/center-for-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d